Intro to immunology Flashcards

1
Q

What does the immune system need to do?

A
  1. detect threat
  2. respond agains threat
  3. minimise collateral damage
  4. remember the threat to respond more effectively if met next time

Do not think of the immune system as a separate entity- it is fully integrated into the body’s systems

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What is the immune system?

A

Complex cellular and protein network that has evolved to protect the host from pathogenic microbes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

Is the immune system involved in homeostasis?

A

YES- tissue repair

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

What happens if the immune system fails?

A

This is known as immunodeficiency disease ( immunodeficiency- SCID (severe combined immunodeficiency)) - leads to increased susceptibility to infection and sometimes cancer.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

What can be the cause of autoimmune conditions?

A

Abnormal function or regulation of the immune system may lead to disease, e.g. autoimmune diseases, allergy

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What is the normal function of the immune system?

A

To identify and eliminate harmful microorganisms and harmful substances such as toxins. It does this by:

  • distinguishing between self and non-self ( abnormal self in the case of cancer)
  • Identifying danger signals, including tissue damage (there must be some secondary danger of inflammatory signal)

The immune system must have a balance between clearing the pathogen and causing collateral damage to the host.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

True/ false- bacteria reproduce faster than viruses?

A

true

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

Examples of vaccinations that have had impact on human health

A

Diptheria, small pox and Polio incidence has dropped considerably since the release of vaccines.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

Evolution race between pathogen and host- what is this?

A

Pathogen and hotst exert selection pressure on each other.

The pathogen reproduces much faster than the host and can EVOLVE faster.

This is why the host has to rely on an immune system which is rapid and adaptive. Our most polymorphic genes (HLA and KIR) are involved in the immune system- this selection is due to exposure of infectious disease.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

There are two strategies that the immune cells used to recognise danger (via receptors)- describe them.

A
  1. Recognise molecular patterns. There hundreds of these types of receptors (small in comparison to the second type) and they are germ line encoded.
  2. Recognise precise structures- there are millions of these receptors and they are made by combining gene segments to generate a HUGE VARIETY of receptors (because of the different combinations)
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

Advantages of the 1st strategy (recognise molecular patterns)

A

Many cells can express the same receptor which increases the chance of it running into the foreign material very quickly- this allows for a rapid and effective response.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Disadvantages of the 1st strategy (recognise molecular patterns)

A

Limited receptor diversity so there is a chance that the receptor is not complimentary to the foreign material. This means that some pathogens will not be recognised

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

Advantages of the 2nd strategy (recognise surface structures)

A

There is a mass diversity with this method- all structures have the potential to be recognised because of the random nature of the generation of receptors.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

Disadvantages of the 2nd strategy (recognise surface structures)

A

There are only a few cells expressed with each receptor so they must be greatly expanded to generate an effective response- this can take time.

There is a chance for autoimmunity due to the random nature of the receptor generation.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

The strategy that recognises molecular patterns has two types of triggers- what are they?

A
  1. PAMPs- pathogen associated molecular patterns
  2. DAMPs- damage associated molecular patterns

(N.B about DAMPs- when cells become damaged, they tend to release their contents)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

Examples of PAMPs

A
  • Flagellin and peptidoglycans (bacteria)
  • dsRNA in cytoplasm (virus)
  • Mannoproteins (fungus)
  • Profilin (parasite)
17
Q

Examples of DAMPs

A
  • Nuclear components
  • Extracellular ATP
  • Heat shock proteins
  • Uric acid

ECM leakage- finding collagens and fibronectins is a sign of tissue damage

18
Q

What are the 2 types of cells in antigen-specific receptors strategy?

A

T cells

B cells

19
Q

What do B cells do?

A

B cells have antigen receptors which are bound to their membrane

They bind INTACT antigens

20
Q

What do T cells do?

A

There are 2 proteins (alpha and beta) expressed on the t cell surface.

They make the T cell receptor (TCR)- binds processed antigen fragments at the cell surface.

21
Q

Describe the specifity of the receptors

A

Each antigen receptor binds to a particular site- an epitope- a different antigen.

Each clone of B cells or T cells has a unique receptor- specific to one antigen- each cell carries many copies of this receptor on the cell surface

22
Q

What is innate immunity?

A

Uses strategy 1

It is independent of previous exposure and depends on pre-formed and rapidly synthesised components (all due to your germ line). Present from birth.

FAST

There is limited specifity- only recognises patterns to do with danger.

23
Q

What is adaptive immunity?

A

Uses strategy 2- Adaptation to exposure. It depends on clonal selection (expansion selected for antigen specifity)

SLOW

Highly specific and gives immunologial memory.

24
Q

What does the innate immune response do?

A
  • destroys invading nucleic acids (viruses)
  • activates inflammatory pathways and signals for recruitment of immune cells. supressess replication
  • elicits type 1 interferons for antiviral defence
  • IT BUYS TIME- promotes and directs the appropriate adaptive immune response.
25
Q

Describe adaptive immunity

A

specific to foreign antigens (usually proteins)- can form memory and requires priming.

It uses cellular immunity - t cells and b cells

Humoral immunity- antibodies

(eosinophils, basophils, dendritic cells, natural killer cells and mast cells kinda fit into both acquired and innate immunity)

26
Q

Which cells are involved in the adaptive immune response?

A

Lymphocytes!- B and T cells (agranular leukoctyes)

T (thymus derived) cells

B (bone marrow derived) cells

Each subset has distinct cell-surface molecules

e.g. CD4 on T helper cells

cytokines and antibodies are the soluble factors

27
Q

What are the main components of the adaptive immune response?

A

Cells:

  • neutrophils
  • macrophages
  • eosinophils

Soluble factors:

  • acute- phase proteins (proteins that respond to inflammatory cytokines)
  • cytokines
  • complement
28
Q

What is the primary response

A

This is the first time that the host has seen the pathogen

29
Q

Describe the stages of this graph

A
  1. initially innate immunity is triggered- there is a rise in type 1 interferon levels which interferes with virus replication
  2. Then natural killer cells are stimulated- they recognise infected cells and lyse them- these responses help to flatten out virus replication (which is why virus conc is decreasing)
  3. The adaptive immune response is now needed to get rid of the virus- this will take a little bit more time
  4. There is now a rise in cytotoxic T lymphocytes (CTLs)- recognise and lyse infected cells.
  5. CTLs start to produce antibodies against the virus
30
Q

Anatomical barriers for innate immunity

A

Skin

Mucus- trapping microbes

Cilial propulsion on epithelia

31
Q

What are the physiological barriers for innate immunity?

A

Low pH

Secretion of lysosomes

Interferons

Anti-microbial peptides

32
Q

What happens to the large number of unique lymphocytes that are produced?

A

Lymphocytes that meet an antigen they recognize will proliferate and survive but there is a huge majority of lymphocyte clones that will die out.

33
Q

What is a naive lymphocyte?

A

lymphocytes which have never come into contact with their antigen before

98% of T cells are in the lymph circulation and organs

2% is in the blood

34
Q

How are naïve lymphocytes activated?

A

An antigen will bind to surface receptors of the B cell (Ig) or T cell (TCR) and cause selective expansion of that clone.

Most of the proliferated lymphocytes will die after fulfilling their function- some will survive as memory cells. re-exposure to a previously encountered antigen leads to a more rapid and greater immune response (secondary response)

35
Q

How does the primary response differ from the secondary response?

A

The lag phase is when you don’t have a response to antigen yet. If a new antigen, will have to go through primary response.